Wetland Aliens Cause Bird Extinction
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Table 7: Species Changing IUCN Red List Status (2014-2015)
IUCN Red List version 2015.4: Table 7 Last Updated: 19 November 2015 Table 7: Species changing IUCN Red List Status (2014-2015) Published listings of a species' status may change for a variety of reasons (genuine improvement or deterioration in status; new information being available that was not known at the time of the previous assessment; taxonomic changes; corrections to mistakes made in previous assessments, etc. To help Red List users interpret the changes between the Red List updates, a summary of species that have changed category between 2014 (IUCN Red List version 2014.3) and 2015 (IUCN Red List version 2015-4) and the reasons for these changes is provided in the table below. IUCN Red List Categories: EX - Extinct, EW - Extinct in the Wild, CR - Critically Endangered, EN - Endangered, VU - Vulnerable, LR/cd - Lower Risk/conservation dependent, NT - Near Threatened (includes LR/nt - Lower Risk/near threatened), DD - Data Deficient, LC - Least Concern (includes LR/lc - Lower Risk, least concern). Reasons for change: G - Genuine status change (genuine improvement or deterioration in the species' status); N - Non-genuine status change (i.e., status changes due to new information, improved knowledge of the criteria, incorrect data used previously, taxonomic revision, etc.); E - Previous listing was an Error. IUCN Red List IUCN Red Reason for Red List Scientific name Common name (2014) List (2015) change version Category Category MAMMALS Aonyx capensis African Clawless Otter LC NT N 2015-2 Ailurus fulgens Red Panda VU EN N 2015-4 -
Nordmann's Greenshank Population Analysis, at Pantai Cemara Jambi
Final Report Nordmann’s Greenshank Population Analysis, at Pantai Cemara Jambi Cipto Dwi Handono1, Ragil Siti Rihadini1, Iwan Febrianto1 and Ahmad Zulfikar Abdullah1 1Yayasan Ekologi Satwa Alam Liar Indonesia (Yayasan EKSAI/EKSAI Foundation) Surabaya, Indonesia Background Many shorebirds species have declined along East Asian-Australasian Flyway which support the highest diversity of shorebirds in the world, including the globally endangered species, Nordmann’s Greenshank. Nordmann’s Greenshank listed as endangered in the IUCN Red list of Threatened Species because of its small and declining population (BirdLife International, 2016). It’s one of the world’s most threatened shorebirds, is confined to the East Asian–Australasian Flyway (Bamford et al. 2008, BirdLife International 2001, 2012). Its global population is estimated at 500–1,000, with an estimated 100 in Malaysia, 100–200 in Thailand, 100 in Myanmar, plus unknown but low numbers in NE India, Bangladesh and Sumatra (Wetlands International 2006). The population is suspected to be rapidly decreasing due to coastal wetland development throughout Asia for industry, infrastructure and aquaculture, and the degradation of its breeding habitat in Russia by grazing Reindeer Rangifer tarandus (BirdLife International 2012). Mostly Nordmann’s Greenshanks have been recorded in very small numbers throughout Southeast Asia, and there are few places where it has been reported regularly. In Myanmar, for example, it was rediscovered after a gap of almost 129 years. The total count recorded by the Asian Waterbird Census (AWC) in 2006 for Myanmar was 28 birds with 14 being the largest number at a single locality (Naing 2007). In 2011–2012, Nordmann’s Greenshank was found three times in Sumatera Utara province, N Sumatra. -
Long-Billed Curlew Distributions in Intertidal Habitats: Scale-Dependent Patterns Ryan L
LONG-BILLED CURLEW DISTRIBUTIONS IN INTERTIDAL HABITATS: SCALE-DEPENDENT PATTERNS RYAN L. MATHIS, Department of Wildlife, Humboldt State University, Arcata, Cali- fornia 95521 (current address: National Wild Turkey Federation, P. O. Box 1050, Arcata, California 95518) MARK A. ColwELL, Department of Wildlife, Humboldt State University, Arcata, California 95521; [email protected] LINDA W. LEEMAN, Department of Wildlife, Humboldt State University, Arcata, California 95521 (current address: EDAW, Inc., 2022 J. St., Sacramento, California 95814) THOMAS S. LEEMAN, Department of Wildlife, Humboldt State University, Arcata, California 95521 (current address: Environmental Science Associates, 8950 Cal Center Drive, Suite 300, Sacramento, California 95826) ABSTRACT. Key ecological insights come from understanding a species’ distribu- tion, especially across several spatial scales. We studied the distribution (uniform, random, or aggregated) at low tide of nonbreeding Long-billed Curlew (Numenius americanus) at three spatial scales: within individual territories (1–8 ha), in the Elk River estuary (~50 ha), and across tidal habitats of Humboldt Bay (62 km2), Cali- fornia. During six baywide surveys, 200–300 Long-billed Curlews were aggregated consistently in certain areas and were absent from others, suggesting that foraging habitats varied in quality. In the Elk River estuary, distributions were often (73%) uniform as curlews foraged at low tide, although patterns tended toward random (27%) when more curlews were present during late summer and autumn. Patterns of predominantly uniform distribution across the estuary were a consequence of ter- ritoriality. Within territories, eight Long-billed Curlews most often (75%) foraged in a manner that produced a uniform distribution; patterns tended toward random (16%) and aggregated (8%) when individuals moved over larger areas. -
The First Record of Far Eastern Curlew (Numenius Madagascariensis) in British Columbia
The First Record of Far Eastern Curlew (Numenius madagascariensis) in British Columbia. By Rick Toochin and Don Cecile. Submitted: April 15, 2018. Introduction and Distribution The Far Eastern Curlew (Numenius madagascariensis) is the largest migratory shorebird in the world. This species is found only along the East Asian–Australasian Flyway. The Far Eastern Curlew breeds on open mossy or transitional bogs, moss-lichen bogs and wet meadows, and on the swampy shores of small lakes in Siberia and Kamchatka in Russia, as well as in north-eastern Mongolia and China (Hayman et al. 1986, del Hoyo et al. 1996). The Yellow Sea of the Republic of Korea and China is a vitally important stopover site on migration. This species is also a common passage migrant in Japan and Indonesia, and is occasionally recorded moving through Thailand, Brunei, Bangladesh, Vietnam, Philippines, Malaysia and Singapore (O’Brien et al. 2006). During the winter a few birds occur in southern Republic of Korea, Japan, China, and Taiwan (Brazil 2009, EAAFP 2017). About 25% of the population is thought to winter in the Philippines, Indonesia and Papua New Guinea. Most birds, approximately 73% or 28,000 individuals, spend the winter in Australia, where birds are found primarily on the coast of all states, particularly the north, east and south-east regions including Tasmania (Bamford et al. 2008, BirdLife 2016). In the early 2000’s, the global population of the Far Eastern Curlew was estimated at 38,000 individuals (BirdLife 2016). Unfortunately due to the fact that the global population is declining, the true population size is likely to be much smaller, and may not exceed 20,000 individuals (BirdLife 2016). -
BIRDCONSERVATION the Magazine of American Bird Conservancy Fall 2016 BIRD’S EYE VIEW a Life Shaped by Migration
BIRDCONSERVATION The Magazine of American Bird Conservancy Fall 2016 BIRD’S EYE VIEW A Life Shaped By Migration The years have rolled by, leaving me with many memories touched by migrating birds. Migrations tell the chronicle of my life, made more poignant by their steady lessening through the years. still remember my first glimmer haunting calls of the cranes and Will the historic development of of understanding of the bird swans together, just out of sight. improved relations between the Imigration phenomenon. I was U.S. and Cuba nonetheless result in nine or ten years old and had The years have rolled by, leaving me the loss of habitats so important to spotted a male Yellow Warbler in with many memories touched by species such as the Black-throated spring plumage. Although I had migrating birds. Tracking a Golden Blue Warbler (page 18)? And will passing familiarity with the year- Eagle with a radio on its back Congress strengthen or weaken the round and wintertime birds at through downtown Milwaukee. Migratory Bird Treaty Act (page home, this springtime beauty was Walking down the Cape May beach 27), America’s most important law new to me. I went to my father for each afternoon to watch the Least protecting migratory birds? an explanation of how I had missed Tern colony. The thrill of seeing this bird before. Dad explained bird “our” migrants leave Colombia to We must address each of these migration, a talk that lit a small pour back north. And, on a recent concerns and a thousand more, fire in me that has never been summer evening, standing outside but we cannot be daunted by their extinguished. -
A Case of the Population Trend of Far Eastern Curlew Numenius Madagascariensis in Banyuasin Peninsula, South Sumatra, Indonesia
Ecologica Montenegrina 44: 11-18 (2021) This journal is available online at: www.biotaxa.org/em http://dx.doi.org/10.37828/em.2021.44.2 Is the global decline reflects local declines? A case of the population trend of Far Eastern Curlew Numenius madagascariensis in Banyuasin Peninsula, South Sumatra, Indonesia MUHAMMAD IQBAL1*, CIPTO DWI HANDONO2, DENI MULYANA3, ARUM SETIAWAN4, ZAZILI HANAFIAH4, HENNI MARTINI5, SARNO4, INDRA YUSTIAN4 & HILDA ZULKIFLI4 1Biology Program, Faculty of Science, Sriwijaya University, Jalan Padang Selasa 524, Palembang, South Sumatra 30139, Indonesia. 2Yayasan Ekologi Satwa Liar Indonesia (EKSAI), Jalan Kutisari 1 No. 19, Surabaya, East Java 60291, Indonesia 3Berbak Sembilang National Park, South Sumatra office, Jalan Tanjung Api-api komplek Imadinatuna No. 114, South Sumatra, Indonesia 4Department of Biology, Faculty of Science, Sriwijaya University, Jalan Raya Palembang-Prabumulih km 32, Indralaya, South Sumatra, Indonesia. 5Hutan Kita Institute (HAKI), Jalan Yudo No. 9H, Palembang, South Sumatra 30126, Indonesia *Corresponding author: [email protected] Received 28 June 2021 │ Accepted by V. Pešić: 13 July 2021 │ Published online 16 July 2021. Abstract Far Eastern Curlew Numenius madagascariensis (Linnaeus, 1766) is Endangered species confined in East Asian Australasian Flyway (EAAF) sites. We compiled and summarized all historical numbers of Far Eastern Curlew in Banyuasin Peninsula, South Sumatra, Indonesia. A total of 30 records were documented from 1984 to 2020. The largest number is 2,620 individuals during the migration period in 1988. Unfortunately, the largest number drop to 1,750 individuals in wintering period in 2008, and then drop to 850 individuals in 2019. The numbers indicate that the population decline by up to 62% in the last 35 years (1984 to 2019). -
Cuba Trip Report Jan 4Th to 14Th
Field Checklist to the Birds of Cuba Cuba Trip Report Jan 4th to 14th 1 Field Checklist to the Birds of Cuba Cuba Bird List Species Scientific Name Seen Heard Order ANSERIFORMES Family Anatidae Ducks, Geese, Swans 1. West Indian Whistling-Duck Dendrocygna arborea • 2. Fulvous Whistling-Duck Dendrocygna bicolor 3. American Wigeon Anas americanas 4. Wood Duck Aix sponsa 5.Blue-winged Teal Anas discors • 6. Northern Shoveler Anas clypeata • 7. White-cheeked Pintail Anas bahamensis 8. Northern Pintail Anas acutas 9. Green-winged Teal Anas carolinensis 10. Ring-necked Duck Aythya collaris 11.Lesser Scaup Aythya affinis 12. Hooded Merganser Lophodytes cucullatus 13. Red-breasted Merganser Mergus serrator 14. Masked Duck Nomonyx dominicus 15. Ruddy Duck Oxyura jamaicensis Order GALLIFORMES Family Phasianidae Pheasant, Guineafowl 16. Helmeted Guineafowl (I) • Family Odontophoridae New World Quail 17. Northern Bobwhite Colinus virginianus cubanensis Order PODICIPEDIFORMES Grebes 18. Least Grebe Tachybaptus dominicus • 19. Pied-billed Grebe Podilymbus podiceps • Order CICONNIIFORMES Family Ciconiidae Storks 20. Wood Stork Mycteria americana 2 Field Checklist to the Birds of Cuba Cuba Bird List Species Scientific Name Seen Heard Order SULIFORMES Family Fregatidae Frigatebirds 21. Magnificent Frigatebird Fregata magnificens • Family Sulidae Boobies, Gannets 22. Brown Booby Sula leucogaster Family Phalacrocoracidae Cormorants 23. Neotropic Cormorant Phalacrocorax brasiliannus • 24. Double-crested Cormorant Phalacrocorax auritus • Family Anhingidae Darters 25. Anhinga Anhinga anhinga • Order PELECANIFORMES Family Pelecanidae Pelicans 26. American White Pelican Pelecanus erythrorhynchos 27. Brown Pelican Pelecanus occidentalis • Family Ardeidae Herons, Bitterns, Allies 28. Least Bittern Ixobrychus exilis • 29. Great Blue Heron Ardea herodias • 30. Great Egret Ardea alba • 31. Snowy Egret Egretta thula • 32. -
The Systematic Position of the Surfbird, Aphriza Virgata
THE SYSTEMATIC POSITION OF THE SURFBIRD, APHRIZA VIRGATA JOSEPH R. JEHL, JR. University of Michigan Museum of Zoology Ann Arbor, Michigan 48104 The taxonomic relationships of the Surfbird, ( 1884) elevated the tumstone-Surfbird unit Aphriza virgata, have long been one of the to family rank. But, although they stated (p. most controversial problems in shorebird clas- 126) that Aphrizu “agrees very closely” with sification. Although the species has been as- Arenaria, the only points of similarity men- signed to a monotypic family (Shufeldt 1888; tioned were “robust feet, without trace of web Ridgway 1919), most modern workers agree between toes, the well formed hind toe, and that it should be placed with the turnstones the strong claws; the toes with a lateral margin ( Arenaria spp. ) in the subfamily Arenariinae, forming a broad flat under surface.” These even though they have reached no consensuson differences are hardly sufficient to support the affinities of this subfamily. For example, familial differentiation, or even to suggest Lowe ( 1931), Peters ( 1934), Storer ( 1960), close generic relationship. and Wetmore (1965a) include the Arenariinae Coues (1884605) was uncertain about the in the Scolopacidae (sandpipers), whereas Surfbirds’ relationships. He called it “a re- Wetmore (1951) and the American Ornithol- markable isolated form, perhaps a plover and ogists ’ Union (1957) place it in the Charadri- connecting this family with the next [Haema- idae (plovers). The reasons for these diverg- topodidae] by close relationships with Strep- ent views have never been stated. However, it silas [Armaria], but with the hind toe as well seems that those assigning the Arenariinae to developed as usual in Sandpipers, and general the Charadriidae have relied heavily on their appearance rather sandpiper-like than plover- views of tumstone relationships, because schol- like. -
Tasmanian Bird Report 38
Tasmanian Bird Report 38 July 2017 BirdLife Tasmania, a branch of BirdLife Australia Editor, Wynne Webber TASMANIA The Tasmanian Bird Report is published by BirdLife Tasmania, a regional branch of BirdLife Australia Number 38 © 2017 BirdLife Tasmania, GPO Box 68, Hobart, Tasmania, Australia 7001 ISSN 0156-4935 This publication is copyright. All rights reserved. No part of this publication may, except for the purposes of study or research, be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, without the prior permission in writing of BirdLife Tasmania or the respective paper’s author(s). Acknowledgments NRM South, through funding from the Australian Government’s National Landcare Programme, has provided financial assistance for the publication of this report. We thank them both for this contribution. Contents Editorial iv Wynne Webber State of Tasmania’s terrestrial birds 2014–15 1 Mike Newman, Nick Ramshaw, Sue Drake, Eric Woehler, Andrew Walter and Wynne Webber Risk of anticoagulant rodenticides to Tasmanian raptors 17 Nick Mooney Oddities of behaviour and occurrence 26 Compiler, Wynne Webber When is the best time to survey shorebirds? 31 Stephen Walsh A Eurasian Coot nests in Hobart 32 William E. Davis, Jr Changes in bird populations on Mt Wellington over a 40-year period 34 Mike Newman 2016 Summer and winter wader counts 44 (incorporating corrected tables for 2015 summer counts) Eric Woehler and Sue Drake Editorial In this Tasmanian Bird Report we institute what is hoped to be a useful and ongoing enterprise, which replaces the systematic lists of earlier years: a report on ‘The state of Tasmania’s birds’. -
Pages 345–366850.31 KB
Conservation Science W. Aust. 8 (3) : 345–366 (2013) Wader numbers and distribution on Eighty Mile Beach, north-west Australia: baseline counts for the period 1981–2003 CLIVE MINTON 1, MICHAEL CONNOR 2, DAVID PRICE 3, ROSALIND JESSOP 4, PETER COLLINS 5, HUMPHREY SITTERS 6, CHRIS HASSELL 7, GRANT PEARSON 8, DANNY ROGERS 9 1 165 Dalgetty Road Beaumaris, Victoria 3193 2 19 Pamela Grove Lower Templestowe, Victoria 3107 [email protected] 3 8 Scattor View Bridford, Exeter, Devon EX6 7JF, UK 4 Phillip Island Nature Park, PO Box 97 Cowes, Victoria 3922 5 214 Doveton Crescent Soldiers Hill, Ballarat, Victoria 3350 6 Higher Wyndcliffe Barline, Beer, Seaton, Devon EX12 3LP, UK 7 PO Box 3089 Broome, Western Australia 6725 8 Western Australian Department of Parks and Wildlife, PO Box 51 Wanneroo, Western Australia 6065 9 340 Ninks Road St Andrews, Victoria 3761 ABSTRACT This paper analyses ground counts and aerial surveys of high-tide wader roosts conducted over the 23-year period from 1981 to 2003, at Eighty Mile Beach, north-west Australia. It provides a baseline data set with which later count data can be compared. Over the study period, Eighty Mile Beach held a maximum of around 470,000 waders in any given year. This represented around 20% of the total number of migratory waders visiting Australia each year and around 6% of the total East Asian – Australasian Flyway migratory wader population. The most numerous species were great knot (169,000), bar-tailed godwit (110,000), greater sand plover (65,000) and oriental plover (58,000). -
Evaluating Threats to New Zealand Seabirds Report for the Department of Conservation
Evaluating threats to New Zealand seabirds Report for the Department of Conservation Authors: Edward Abraham Yvan Richard Katherine Clements PO Box 27535, Wellington 6141 New Zealand dragonfly.co.nz Cover Notes To be cited as: Abraham, Edward; Yvan Richard; Katherine Clements (2016). Evaluating threats to New Zealand seabirds, 19 pages. Report for the Department of Conservation. Crown copyright © This report is licensed for re-use under a Creative Commons Aribution 3.0 New Zealand Licence. This allows you to distribute, use, and build upon this work, provided credit is given to the original source. Cover image: hps://www.flickr.com/photos/4nitsirk/16121373851 EXECUTIVE SUMMARY The New Zealand Department of Conservation is developing a seabird threat framework, “to beer understand, and manage, at-sea threats to our seabirds”. This framework will allow the impact of threats on seabird populations to be qualitatively assessed, and will be used to prioritise a programme of seabird population monitoring. As a first stage in developing the framework, a database of demographic parameters and threats was prepared. In this project, a process was estab- lished for reviewing and synthesising this information. The demographic parameters were then used to develop an online tool, which allowed for the impact of changes in parameters on population growth rates to be assessed. In the future, this tool will allow the impact of current and potential threats on seabird populations to be promptly explored. The process was trialled on the 12 albatross taxa recognised -
European Red List of Birds
European Red List of Birds Compiled by BirdLife International Published by the European Commission. opinion whatsoever on the part of the European Commission or BirdLife International concerning the legal status of any country, Citation: Publications of the European Communities. Design and layout by: Imre Sebestyén jr. / UNITgraphics.com Printed by: Pannónia Nyomda Picture credits on cover page: Fratercula arctica to continue into the future. © Ondrej Pelánek All photographs used in this publication remain the property of the original copyright holder (see individual captions for details). Photographs should not be reproduced or used in other contexts without written permission from the copyright holder. Available from: to your questions about the European Union Freephone number (*): 00 800 6 7 8 9 10 11 (*) Certain mobile telephone operators do not allow access to 00 800 numbers or these calls may be billed Published by the European Commission. A great deal of additional information on the European Union is available on the Internet. It can be accessed through the Europa server (http://europa.eu). Cataloguing data can be found at the end of this publication. ISBN: 978-92-79-47450-7 DOI: 10.2779/975810 © European Union, 2015 Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Printed in Hungary. European Red List of Birds Consortium iii Table of contents Acknowledgements ...................................................................................................................................................1 Executive summary ...................................................................................................................................................5 1.